Canonical Allele Identifier: CA1728106778
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388598G= , CM000669.2:g.97388598G= GRCh38
NC_000007.13:g.97017910G= , CM000669.1:g.97017910G= GRCh37
NC_000007.12:g.96855846G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59951C=